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Clinical Trials/NCT01197326
NCT01197326
Completed
Not Applicable

The Use of IntelliVue Patient Monitor MP5 Rel. G.1 for the Prevention of "Failure to Rescue" Using Early Warning Score

Philips Healthcare1 site in 1 country414 target enrollmentAugust 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sepsis
Sponsor
Philips Healthcare
Enrollment
414
Locations
1
Primary Endpoint
Survival
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to assess if, compared with standard paper-based systems, an automated Early Warning System (EWS) resident in a spot check patient monitor, can help to identify deteriorating patients.

Detailed Description

The purpose of this study is to assess if, compared with standard paper-based systems, an automated Early Warning System (EWS) resident in a spot check patient monitor, can help to identify patients in the acute care settings but outside of the intensive care unit, who may be experiencing physiological instability and who are in need of rapid clinical intervention by a Rapid Response Team (RRT)/ Medical Emergency Team (MET). The development of such an automated system by offers a unique opportunity to assess its user-friendliness, labour-saving effect, feasibility and clinical utility. Accordingly, we plan to conduct a research program aimed at assessing this new approach toward patient monitoring. This study will use the hospital's Standard of Care protocol for the monitoring of vital signs (including timing and vital signs collected) and a commercially available automatic spot check monitor to collect data. No investigational procedures or devices are associated with this protocol.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
June 2010
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • all patients admitted to the study units during the period of data collection

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Survival

Time Frame: 6 months

Survival at the end of the RRT call (time when the RRT team left the patient, average duration of calls around 25 min)

Secondary Outcomes

  • Respiration Rate Impact on RRT Calls(6 months)

Study Sites (1)

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